Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH

Genome Research

Volumn 21, Issue 4, 2011, Pages 535-544

  Neill, Nicholas J ^a   Ballif, Blake C ^a   Lamb, Allen N ^a   Parikh, Sumit ^b   Ravnan, J Britt ^a   Schultz, Roger A ^a   Torchia, Beth S ^a   Rosenfeld, Jill A ^a   Shaffer, Lisa G ^a  

^a PerkinElmer   (United States)

^b LERNER RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

METHYL CPG BINDING PROTEIN 2;

ARTICLE; CHROMOSOME BREAKAGE; CHROMOSOME DUPLICATION; CHROMOSOME INSERTION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GENE DISRUPTION; GENE DOSAGE; GENETIC VARIABILITY; HUMAN; INHERITANCE; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; RETT SYNDROME;

BASE SEQUENCE; CHROMOSOME BREAKPOINTS; CHROMOSOMES, HUMAN; COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; FEMALE; GENE ORDER; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MOLECULAR SEQUENCE DATA; MUTAGENESIS, INSERTIONAL; RETT SYNDROME; SEQUENCE ALIGNMENT; TRANSLOCATION, GENETIC;

EID: 79952222136     PISSN: 10889051     EISSN: 15495469     Source Type: Journal    
DOI: 10.1101/gr.114579.110     Document Type: Article

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